Consider the reaction below: Br H₂O heat OH to 1. The reaction mechanism for the reaction is choose your answer... 2. The nucleophile in the reaction is a choose your answer... ✓nucleophile.
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- Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- Rate = k [CH3CH2Br][CH3COO-] Which mechanism would best fit the data?Identify which substitution mechanism best fits the following statement: The reaction proceeds through a concerted mechanism. A) SN1 B) SN2Show the steps of the next reaction in detail. And explain why it's hard to go along with the dotted line.
- For the reaction scheme below: (a) Suggest a reagent X that could be used to accomplish the first step. (b) Draw the curly arrow mechanism for the second step in the scheme.Give 3 examples of a reaction mechanism of E1 that follows Zaitsev's rule.For the reduction of 2-methyl cyclohexanone to methyl cyclohexanol using NaBH4... 1. What is the reaction mechanism (draw curved arrows)? What is the nucleophile? Electrophile? 2. Using your reaction mechanism from the above question, sketch the reaction coordinatediagram. What does the transition state most likely look like? What is the rate-determining step?
- Complete the reactions given below, write down the type of mechanism (SN1, SN2, E1, E2)?What would the mechanism look like for the reaction below?For SN1 Explain the order in which 1o (primary) alkyl halides reacted (fastest to slowest) and explain why. The 1o primary alkyl halides are: (see picture below) 1-chlorobutane 1-bromobutane 1-chloro-2butene benzylchloride